| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:75639263-75639568 | Rare:60 | ||||
| chr17:75639925-75640161 | Common:1; Rare:58 | ||||
| chr17:75646091-75646428 | Common:5; Rare:75 | ||||
| chr17:75667136-75667474 | Common:5; Rare:112 | ||||
| chr17:75721179-75721612 | Common:3; Rare:131; Clinvar:3 | ||||
| chr17:75727400-75727756 | Rare:126; Clinvar:2; Clinvar (pathogenic):2 | ||||
| chr17:75784555-75784877 | Common:2; Rare:145 | ||||
| chr17:75843734-75843824 | Rare:23 | ||||
| chr17:75844695-75845017 | Common:1; Rare:63; Clinvar:1 | ||||
| chr17:75855269-75855699 | Common:1; Rare:122 | ||||
| chr17:75878562-75878792 | Common:3; Rare:70 | ||||
| chr17:75904860-75905218 | Common:4; Rare:100 | ||||
| chr17:75978954-75979339 | Rare:106; Clinvar:4; Clinvar (benign):1 | ||||
| chr17:75979348-75979586 | Common:1; Rare:71; Clinvar (benign):1 | ||||
| chr17:76072487-76072661 | Rare:53 |